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rs104894361

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104894361(A;T)
Make rs104894361(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position25245370
GeneKRAS
is asnp
is mentioned by
dbSNPrs104894361
ebirs104894361
HLIrs104894361
Exacrs104894361
Varsomers104894361
Maprs104894361
PheGenIrs104894361
hapmaprs104894361
1000 genomesrs104894361
hgdprs104894361
ensemblrs104894361
gopubmedrs104894361
geneviewrs104894361
scholarrs104894361
googlers104894361
pharmgkbrs104894361
gwascentralrs104894361
openSNPrs104894361
23andMers104894361
23andMe allrs104894361
SNP Nexus

SNPshotrs104894361
SNPdbers104894361
MSV3drs104894361
GWAS Ctlgrs104894361
Max Magnitude0
OMIM190070
Desc
Variant0017
Relatedalso
ClinVar
Risk rs104894361(T;T)
Alt rs104894361(T;T)
Reference rs104894361(A;A)
Significance Pathogenic
Disease Cardiofaciocutaneous syndrome 2 not provided
Variation info
Gene KRAS
CLNDBN Cardiofaciocutaneous syndrome 2 not provided
Reversed 1
HGVS NC_000012.11:g.25398304T>A
CLNSRC HGMD OMIM Allelic Variant
CLNACC RCV000013425.24, RCV000153427.3,